FDA UDI In Commercial Distribution 🇺🇸 United States

myONE M21/60F

DI: 00726893511019 · Model: MYONE-M21/60F-12 · GLOBAL PROTECTION CORP.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
myONE M21/60F
Primary DI
00726893511019
Version / Model
MYONE-M21/60F-12
Company Name
GLOBAL PROTECTION CORP.
Labeler DUNS
364614362
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2023-03-28
Public Version
2
Public Version Date
2023-10-30
Public Version Status
Update
Public Device Record Key
12420519-a6af-4d28-94d0-744625eff550

Device Description

12 Lubricated Latex Condoms

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HIS Condom

GMDN Terms

Code Name
45138 Basic male condom, Hevea-latex

Identifiers

Type ID
Unit of Use 80726893511015
Primary 00726893511019